Vitiligo type cutaneous manifestation of chronic graft-versus-host disease. Case report
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Keywords

Chronic Cutaneous Graft-Versus-Host Disease
Hematopoietic Stem Cell Transplantation
Vitiligo
Dermatology
Immunology
Graft vs Host Disease

How to Cite

1.
Gálvez K, Muñoz P, Vera V, Arce C. Vitiligo type cutaneous manifestation of chronic graft-versus-host disease. Case report. Andes pediatr [Internet]. 2018 Mar. 27 [cited 2026 Apr. 14];89(1):113-7. Available from: https://andespediatrica.cl/index.php/rchped/article/view/395

Abstract

Introduction: Graft-versus-host disease (GVHD) is caused by a pathologic and destructive response of the organism as a result of the interaction between donor immunocompetent T lymphocytes and the recipient tisular antigens. It´s considered the most serious complication of hematopoietic stem cell transplantation, most frequently described after bone marrow transplantation (BMT). The skin is usually the first and most commonly affected organ, in both acute and chronic, with a variable clinical spectrum of presentation.

Objective: To report a case of vitiligo as a manifestation of cutaneous chronic GVHD, a low prevalence sign, which recognition could help to suspect this severe complication.

Case Report: 8 years old male, diagnosed with acute lymphoblastic leukemia (ALL) at 3 years old, had a combined medullary and central nervous system (NCS) relapse with minimal positive disease 3 years afterwards. After 4 years ALL was diagnosed, he received an allogeneic bone marrow transplant. Seven months after the BMT he presented multiple melanocytic nevi with peripheral hypopigmentation, and some isolated asymptomatic, confluent achromic macules on the face, trunk and limbs. The skin biopsy was compatible with chronic vitiligo and sclerodermiform type GVHD. He received topical treatment with Tacrolimus, achieving clinical stabilization.

Conclusions: GVHD leads to the appearance of autoantibodies that could act as a trigger in the onset of autoimmune diseases, such as vitiligo. Consequently it could explain this poorly described manifestation in the literature of chronic cutaneous GVHD.

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